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A first-principles study on stabilizing disordered LiNi0.5Mn1.5O4 cathode material by doping

兴奋剂 阴极 材料科学 结晶学 凝聚态物理 工程物理 化学工程 纳米技术 化学 物理化学 物理 光电子学 工程类
作者
Chih‐Lung Lin,Shih‐kang Lin
出处
期刊:Journal of energy storage [Elsevier]
卷期号:83: 110637-110637
标识
DOI:10.1016/j.est.2024.110637
摘要

High-voltage LiNi0.5Mn1.5O4 (LNMO) is a promising cathode material for high energy-density Li-ion batteries. The LNMO phase exhibits either ordered or disordered structure; meanwhile, the Mn ions possess 3+ and 4+ mixed valence states. The main challenges of LNMO cathode material for real applications are that the ordered LNMO phase possesses poor rate capability and that the Mn3+/4+ redox reaction leads to Mn dissolution. Doping has been a straightforward approach to address these issues, by enhancing the stability of the disordered LNMO phase and reducing the Mn3+ fraction in LNMO. However, experimental trials involved different setups and uncertainties, which usually cannot be directly compared, and thus an investigation of doping influence on disordered LNMO based on fair comparison is required. Herein, we screened and proposed the best dopants that can improve LNMO performance, and we clarified the corresponding mechanism based on first-principles calculations and thermodynamics. The stable doping systems and preferred doping sites were obtained through phase stability evaluation. Mechanism of disordered LNMO stabilization was obtained through analyzing the relation between the change of transition metal valence states after doping and the ability of dopants to stabilize disordered LNMO. It was found that not only extra-electron dopants stabilize disordered LNMO, as most of the studies reported, but extra-hole dopants could also stabilize disordered LNMO. Furthermore, considering the Mn3+/4+ redox reaction, extra-hole dopants, including Mg, Na, and Zn, were suggested to be the dopants that could improve LNMO performance with simultaneously increasing the fraction of disordered phase and avoiding Mn3+/4+ redox reaction.
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